A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv28n21



Internal ID22766220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:233579185..233599722hg38UCSC Ensembl
chr1:233714931..233735468hg19UCSC Ensembl
chr1:231781554..231802091hg18UCSC Ensembl
chr1:230021666..230042203hg17UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg3820538
hg1920538
hg1820538
hg1720538
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv525793, nsv523182
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv28n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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